Variant #0000965807 (NC_000010.10:g.72360387G>A, NM_005041.4:c.272C>T (PRF1))
| Chromosome |
10 |
| Allele |
Unknown |
| Affects function (as reported) |
Effect unknown |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
VUS |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.72360387G>A |
| DNA change (hg38) |
- |
| Published as |
PRF1(NM_001083116.1):c.272C>T (p.(Ala91Val)), PRF1(NM_001083116.3):c.272C>T (p.A91V), PRF1(NM_005041.5):c.272C>T (p.A91V) |
| ISCN |
- |
| DB-ID |
PRF1_000012 See all 4 reported entries |
| Variant remarks |
VKGL data sharing initiative Nederland |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
CLASSIFICATION record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0.02944 View details |
| Owner |
VKGL-NL_VUmc |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_VUmc |
| Date created |
2024-02-26 20:06:56 +01:00 (CET) |
| Date last edited |
2025-05-05 21:14:00 +02:00 (CEST) |

Variant on transcripts
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